Journal of Medicinal Chemistry
Volume 40, Issue 14 (July 4, 1997)
Copyright © 1997
American Chemical Society
2111-2112 | Exceptionally Potent Antispermatogenic Compounds from 8-Halogenation of (4aRS,5SR,9bRS)-Hexahydroindeno[1,2-c]pyridines
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2113-2116 | Inhibition of Human Telomerase by a G-Quadruplex-Interactive Compound
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2117-2122 | (S)-(+)-4-[7-(2,2-Dimethyl-1-oxopro- poxy)-4-methyl-2-[4-[2-(1-piperidinyl)- ethoxy]phenyl]-2H-1-benzopyran-3-yl]- phenyl 2,2-Dimethylpropanoate (EM-800): A Highly Potent, Specific, and Orally Active Nonsteroidal Antiestrogen
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2123-2125 | (1,2,3,4)-1,2-Bis[[N-propyl-N-(4-phen- oxybenzyl)amino]carbonyl]cyclobutane- 3,4-dicarboxylic Acid (A-87049): A Novel Potent Squalene Synthase Inhibitor
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2126-2132 | 5,6-cis-Penems: Broad-Spectrum Anti-Methicillin-Resistant Staphylococcus aureus -Lactam Antibiotics
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2133-2139 | Discovery of Prototype Peptidomimetic Agonists at the Human Melanocortin Receptors MC1R and MC4R
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2140-2147 | Further Definition of the D1 Dopamine Receptor Pharmacophore: Synthesis of trans-6,6a,7,8,9,13b-Hexahydro-5H-benzo[d]naphth[2,1-b]azepines as Rigid Analogues of -Phenyldopamine
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2148-2155 | Structural Model of a Cyclic Dynorphin A Analog Bound to Dodecylphosphocholine Micelles by NMR and Restrained Molecular Dynamics
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2156-2163 | Substituted 3-(Phenylsulfonyl)-1-phenylimidazolidine-2,4-dione Derivatives as Novel Nonpeptide Inhibitors of Human Heart Chymase
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2164-2176 | Potent HIV Protease Inhibitors Containing a Novel (Hydroxyethyl)amide Isostere
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2177-2183 | A Facile, Alternative Synthesis of 4'-Thioarabinonucleosides and Their Biological Activities
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2184-2190 | Synthesis and Cellular Uptake of 2'-Substituted Analogues of (E)-5-(2-[125I]Iodovinyl)-2'-deoxyuridine in Tumor Cells Transduced with the Herpes Simplex Type-1 Thymidine Kinase Gene. Evaluation as Probes for Monitoring Gene Therapy
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2191-2195 | Phosphodiester Amidates of Unsaturated Nucleoside Analogues: Synthesis and Anti-HIV Activity
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2196-2210 | Potent Tetracyclic Guanine Inhibitors of PDE1 and PDE5 Cyclic Guanosine Monophosphate Phosphodiesterases with Oral Antihypertensive Activity
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2211-2216 | Iron-Mediated Generation of the Neurotoxin 6-Hydroxydopamine Quinone by Reaction of Fatty Acid Hydroperoxides with Dopamine: A Possible Contributory Mechanism for Neuronal Degeneration in Parkinson's Disease
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2217-2227 | Steroidal Affinity Labels of the Estrogen Receptor. 3. Estradiol 11-n-Alkyl Derivatives Bearing a Terminal Electrophilic Group: Antiestrogenic and Cytotoxic Properties
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2228-2240 | Design of a Potent Combined Pseudopeptide Endothelin-A/Endothelin-B Receptor Antagonist, Ac-DBhg16-Leu-Asp-Ile-[NMe]Ile-Trp21 (PD 156252): Examination of Its Pharmacokinetic and Spectral Properties
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2241-2251 | Lanthionine-Somatostatin Analogs: Synthesis, Characterization, Biological Activity, and Enzymatic Stability Studies
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2252-2258 | A Refined Model for the Somatostatin Pharmacophore: Conformational Analysis of Lanthionine-Sandostatin Analogs
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2259-2265 | Conformational Dynamics of Thyroid Hormones by Variable Temperature Nuclear Magnetic Resonance: The Role of Side Chain Rotations and Cisoid/Transoid Interconversions
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2266-2275 | Antitumor Agents. 174. 2',3',4',5,6,7-Substituted 2-Phenyl-1,8-naphthyridin-4-ones: Their Synthesis, Cytotoxicity, and Inhibition of Tubulin Polymerization
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2276-2286 | Synthesis and Cytotoxic Evaluation of Substituted Sulfonyl-N-hydroxyguanidine Derivatives as Potential Antitumor Agents
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2287-2287 | A Lifetime of Synergy with Theory and Experiment By Andrew Streitwieser. In Profiles, Pathways and Dreams. Series Editor Jeffrey I. Seeman. American Chemical Society, Washington, DC. 1997. xxvii + 310 pp. 15.5 × 23.5 cm. ISBN O-8412-1836-6. $24.95.
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2287-2287 | Medicinal Chemistry: Today and Tomorrow Edited by Mikio Yamazaki. Blackwell Science Ltd., Oxford. 1997. x + 278 pp. 19.5 × 28 cm. ISBN 0-632-04272-9. $99.95.
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2288-2288 | Water Soluble Furoxan Derivatives as NO Prodrugs
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